High-throughput oncogene mutation detection in human cancer
High-throughput oncogene mutation detection in human cancer
批准号:
7238913
负责人:
Levi A. Garraway
金额:
$17.1万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-01 至 2009-07-31
关键词:
AddressAdmixtureAffectAnatomyBiologicalBiological AssayCancer Gene MutationClassificationClinicalClinical Trials DesignCollectionCompatibleConditionDNADataDiagnosticDideoxy Chain Termination DNA SequencingDiseaseEngineeringEpidermal Growth Factor ReceptorEpithelialFreezingGastrointestinal Stromal TumorsGenesGeneticGenomeGenomicsGenotypeGleevecGoalsGrantHumanIn SituIndividualInterceptMalignant NeoplasmsMass Spectrum AnalysisMethodsMinorMolecularMolecular EpidemiologyMutationMutation DetectionNumbersOncogene ProteinsOncogenesOncogenicParaffinParaffin EmbeddingParaffin TissuePatientsPhasePloidiesPoint MutationProteinsRefractoryResearch PersonnelSamplingSomatic MutationStratificationTechnologyTestingTherapeuticTherapy Clinical TrialsTimeTissuesTumor Suppressor GenesTumor TissueTumor-Derivedabl Oncogeneanticancer researchbasecancer geneticscancer therapycostdesigngain of function mutationgenotyping technologyinsertion/deletion mutationoncologyprogramstherapeutic targettooltumor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): ' Cancer represents a disease of the genome; each tumor harbors a distinct set of mutations that activate oncogenes and inactivate tumor suppressor genes. In the era of targeted therapeutics, it is expected that cancer treatment decisions will increasingly be made based on tumor genetic composition as opposed to tissue of origin. However, most molecular diagnostics that detect cancer gene mutations are expensive, informative for only a single genetic locus, and adversely affected by degraded or stromally admixed genomic DNA. Thus, despite the promise of somatic cancer genetics, at the present time it remains impractical to identify critical oncogene mutations on a large scale and in a manner compatible with routine clinical use. To address these limitations, this application aims to adapt a high-throughput, mass spectrometry- based genotyping technology to detect somatic mutations in a large panel of cancer genes.' In the R21 phase, a platform based on SequenomTM iPLEX genotyping will be developed that interrogates over 600 point mutations (or small insertions/deletions) across 50 oncogenes and selected tumor genes. This platform will also be optimized for cancer gene mutation detection in genomic DNA from paraffin-embedded tumor tissue. In the R33 phase, test the feasibility of this mutation detection approach will be demonstrated in a study of a large and diverse tumor collection. Here, high-throughput oncogene mutation detection will be performed on nearly 2,700 frozen and paraffin-embedded tumors spanning many lineages, including several that have not undergone prior genomic characterization. The ability to perform high-throughput mutation detection in clinical tumor samples will enable unprecedented molecular analyses applicable to molecular epidemiology and translational oncology, including patient stratification for targeted cancer therapeutic trials. These studies therefore offer immense potential to benefit investigators and patients alike on the path to rational cancer therapeutics.
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依托单位:
海外基金